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APOA2 antibody (AA 1-101)

The Mouse Monoclonal anti-APOA2 antibody has been validated for WB, IHC (p) and EIA. It is suitable to detect APOA2 in samples from Human.
Catalog No. ABIN614396

Quick Overview for APOA2 antibody (AA 1-101) (ABIN614396)

Target

See all APOA2 Antibodies
APOA2 (Apolipoprotein A-II (APOA2))

Reactivity

  • 77
  • 33
  • 14
  • 8
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 75
  • 11
  • 9
  • 2
  • 2
  • 1
Mouse

Clonality

  • 81
  • 19
Monoclonal

Conjugate

  • 51
  • 13
  • 10
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This APOA2 antibody is un-conjugated

Application

  • 60
  • 43
  • 29
  • 25
  • 19
  • 13
  • 13
  • 12
  • 9
  • 6
  • 6
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Clone

1H6
  • Binding Specificity

    • 20
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 1-101

    Specificity

    Recognizes Apolipoprotein AII (APOA2).

    Cross-Reactivity (Details)

    Species reactivity (tested):Human.

    Purification

    Protein A Chromatography

    Immunogen

    APOA2 (AAH05282, 1 a.a. ~ 101 a.a) full-length recombinant protein with GST tag.

    Isotype

    IgG1
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Buffer

    PBS, pH 7.2

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    -20 °C

    Storage Comment

    Store the antibody (in aliquots) at -20 °C.
  • Target

    APOA2 (Apolipoprotein A-II (APOA2))

    Alternative Name

    Apolipoprotein A II (Apo AII)

    Background

    Apolipoprotein A II is the second most abundant protein of the high density lipoprotein particles. The apolipoprotein A II gene consists of 4 exons and 3 introns. The four exons encode the 5' untranslated region, pre peptide, a short N terminal domain and a C terminal domain composed of a variable number of lipid binding amphipathic helices. Familial apolipoprotein A II deficiency may result from a splice junction alteration which blocks splicing of intron 3 from the primary transcript and result in the formation of a non functional mRNA.Synonyms: APOA2, Apo-AII, ApoA-II, Apolipoprotein A-II, Apolipoprotein A2

    Gene ID

    336

    NCBI Accession

    NP_001634

    UniProt

    P02652

    Pathways

    Regulation of Lipid Metabolism by PPARalpha, Production of Molecular Mediator of Immune Response, Negative Regulation of Transporter Activity, Lipid Metabolism
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